Albert J. DelMonte

Bristol-Myers Squibb (United States) — United States

Chemistry · Physical Sciences

13h-index877citations38works8.02yr avg
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Research Topics

Cyclopropane Reaction Mechanisms(7), Catalytic C–H Functionalization Methods(6), Crystallization and Solubility Studies(6), X-ray Diffraction in Crystallography(6), Chemical Synthesis and Analysis(4)

Publications38 total

Streamlined Three-Step Telescope Enabled by a Nonaqueous Suzuki–Miyaura Cross-Coupling Reaction
Organic Process Research & Development·2024· 8 cited
CCDC 2210684: Experimental Crystal Structure Determination
The Cambridge Structural Database·2022Open Access
CCDC 2210683: Experimental Crystal Structure Determination
The Cambridge Structural Database·2022Open Access
CCDC 2210685: Experimental Crystal Structure Determination
The Cambridge Structural Database·2022Open Access
Coupling-Condensation Strategy for the Convergent Synthesis of an Imidazole-Fused 2-Aminoquinoline NLRP3 Agonist
The Journal of Organic Chemistry·2022· 12 cited
Pd-Catalyzed Chemoselective O-Benzylation of Ambident 2-Quinolinone Nucleophiles
ACS Catalysis·2022· 11 citedOpen Access
CCDC 2180917: Experimental Crystal Structure Determination
The Cambridge Structural Database·2022Open Access
A Metal-Free Reductive N-Alkylation of Indoles with Aldehydes
Organic Letters·2021· 13 cited
Mechanistic Studies of a Pd-Catalyzed Direct Arylation En Route to Beclabuvir: Dual Role of a Tetramethylammonium Cation and an Unusual Turnover-Limiting Step
ACS Catalysis·2021· 11 cited
Development of a Scalable Negishi Cross-Coupling Process for the Preparation of 2-Chloro-5-(1-(tetrahydro-2<i>H</i>-pyran-2-yl)-1<i>H</i>-pyrazol-5-yl)aniline
Organic Process Research & Development·2020· 5 cited
Pd- and Ni-Based Systems for the Catalytic Borylation of Aryl (Pseudo)halides with B<sub>2</sub>(OH)<sub>4</sub>
The Journal of Organic Chemistry·2020· 41 cited
Development and Scale‐Up of a Palladium‐Catalyzed Intramolecular Direct Arylation in the Commercial Synthesis of Beclabuvir
2020· 3 cited
Safe Scale-up of an Oxygen-Releasing Cleavage of Evans Oxazolidinone with Hydrogen Peroxide
Organic Process Research & Development·2020· 10 citedOpen Access
Cerium(III) Chloride-Mediated Stereoselective Reduction of a 4-Substituted Cyclohexanone Using NaBH<sub>4</sub>
Organic Process Research & Development·2019· 10 cited
Rapid Development of a Commercial Process for Linrodostat, an Indoleamine 2,3-Dioxygenase (IDO) Inhibitor
Organic Process Research & Development·2019· 35 cited
Revisiting the Cleavage of Evans Oxazolidinones with LiOH/H<sub>2</sub>O<sub>2</sub>
Organic Process Research & Development·2019· 25 cited
Direct Lewis Acid Catalyzed Conversion of Enantioenriched <i>N</i>-Acyloxazolidinones to Chiral Esters, Amides, and Acids
The Journal of Organic Chemistry·2018· 37 cited
The First Kilogram Synthesis of Beclabuvir, an HCV NS5B Polymerase Inhibitor
Organic Process Research & Development·2018· 50 cited
Development of Transition Metal-Mediated Cyclopropanation Reactions
Topics in organometallic chemistry·2017· 7 cited
Chemistry in the Pharmaceutical Industry
2017
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Frequent Co-authors

Eric M. Simmons(10), Jason M. Stevens(8), Andrew W. Glace(7), Victor W. Rosso(7), Robert E. Waltermire(6), Bahar Inankur(6), Sha Lou(6), Jeffrey Nye(6), Neil A. Strotman(6), Matthew W. Haley(5), Yichen Tan(5), James Chadwick(5), Peng Geng(5), Brian Lingfeng He(5), Candice L. Joe(5), Sergei Kolotuchin(5), Kevin P. Girard(5), Elisabeth Corbett(4), Zhinong Gao(4), Stéphane Gingras(4)